VEYVONDI 1300 IU powder and solvent for solution for injection.
Sponsors
Baxalta Innovations GmbH, Takeda Development Center Americas Inc., F. Hoffmann-La Roche AG
Conditions
Hereditary severe von Willebrand Disease in childrenType 3 Von Willebrand Diseasesevere von Willebrand Disease
Phase 3
A Phase 3, Prospective, Multicenter, Uncontrolled, Open-Label Clinical Study to Determine the Efficacy, Safety, and Tolerability of rVWF with or without ADVATE in the Treatment and Control of Bleeding Episodes, the Efficacy and Safety of rVWF in Elective and Emergency Surgeries, and the Pharmacokinetics (PK) of rVWF in Children Diagnosed with Severe von Willebrand Disease
RecruitingCTIS2023-509769-18-00
Start: 2017-03-15Target: 8Updated: 2025-12-15
A Phase 3, Prospective, Open-label, Uncontrolled, Multicenter Study on Efficacy and Safety of Prophylaxis with Vonicog Alfa (rVWF) in Children Diagnosed With Severe von Willebrand disease.
RecruitingCTIS2023-509877-22-00
Start: 2024-10-30Target: 11Updated: 2026-01-19
A Phase III, Multicenter, Open-Label Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Emicizumab Prophylaxis in Patients with Type 3 Von Willebrand Disease
RecruitingCTIS2024-515622-80-00
Start: 2025-06-04Target: 47Updated: 2025-06-27